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Antimutagenic and anticarcinogenic effect of methanol extracts of Petasites japonicus Maxim leaves

机译:日本Petasites Maxim叶片甲醇提取物的抗突变和抗癌作用。

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摘要

The methanol extract from the leaves of Petasites japonicus Maxim (PJ) was studied for its (anti-)mutagenic effect with the SOS chromotest and reverse mutation assay. The (anti-)carcinogenic effects were evaluated by the cytotoxicity on human cancer line cells and by the function and the expression of gap junctions in rat liver epithelial cell. PJ extracts significantly decreased spontaneous β-galactosidase activity and β-galactosidase activity induced by a mutagen, ICR, in Salmonella (S.) typhimurium TA 1535/pSK 1002. All doses of the extract (0.08-100 mg/plate) decreased the reversion frequency induced by benzo (α)pyrene (BaP) in S. typhimurium TA 98. It decreased not only the spontaneous reversion frequency but also that induced by BaP in S. typhimurium TA 100. PJ extract showed greater cytotoxic effects on human stomach, colon and uterus cancer cells than on other cancer cell types and normal rat liver epithelial cells. Dye transfers though gap junctions were significantly increased by PJ extracts at concentrations greater than 200 µg/mL and the inhibition of dye transfer by 12-O-tetradecanoylphorobol-13-acetate (TPA) was obstructed in all concentrations of PJ. PJ significantly increased the numbers of gap junction protein connexin 43, and increased the protein expression decreased by TPA in a dose-dependent manner. Based on these findings, PJ is suggested to contain antimutagenic and anticarcionogenic compounds.
机译:用SOS显色法和反向突变试验研究了日本Petaites japonicus Maxim(PJ)叶片中的甲醇提取物的(抗)致突变作用。通过对人癌细胞系的细胞毒性以及大鼠肝上皮细胞中间隙连接的功能和表达来评估(抗)致癌作用。在鼠伤寒沙门氏菌TA 1535 / pSK 1002中,PJ提取物显着降低了由诱变剂ICR诱导的自发β-半乳糖苷酶活性和β-半乳糖苷酶活性。所有剂量的提取物(0.08-100 mg /板)均可降低逆转。鼠伤寒沙门氏菌TA 98中苯并(α)re(BaP)诱导的频率。它不仅降低了鼠伤寒沙门氏菌TA 100中的自发逆转频率,而且降低了BaP诱导的逆转频率。PJ提取物对人的胃,结肠具有更大的细胞毒性作用和子宫癌细胞比其他类型的癌细胞和正常大鼠的肝上皮细胞要多。在大于200 µg / mL的浓度下,PJ提取物通过缝隙连接处的染料转移显着增加,并且在所有浓度的PJ中都阻碍了12-O-十四烷酰基phorobol-13-乙酸盐(TPA)对染料的转移抑制作用。 PJ显着增加了间隙连接蛋白连接蛋白43的数量,并增加了TPA降低的蛋白表达,呈剂量依赖性。基于这些发现,建议PJ包含抗突变和抗癌的化合物。

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